FDA.reportPublic FDA data

IT RADIANT MULTIPLE CC FOR MAN

Manufacturer
F&CO Co., Ltd.
Effective date
2014-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:35:30

Label at a glance#

ProductIT RADIANT MULTIPLE CC FOR MAN
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, OCTISALATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethylhexyl Methoxycinnamate 7.0%, Titanium Dioxide 6.97%, Ethylhexyl Salicylate 3.0%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water, Cyclopentasiloxane, Dipropylene Glycol, Glycerin, Polymethylsilsesquioxane, Niacinamide, Butylene Glycol Dicaprylate/Dicaprate, Octyldodecanol, Glyceryl Stearate, Dicaprylyl Carbonate, Pentylene Glycol, PEG-100 Stearate, Silica, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Potassium Cetyl Phosphate, Iron Oxides (CI 77492), Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Phenoxyethanol, Triceteareth-4 Phosphate, Glycol Stearate, Carbomer, Triethanolamine, PEG-2 Stearate, Aluminum Hydroxide, Stearic Acid, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate, Squalane, Mica (CI 77019), Iron Oxides (CI 77491), Triethoxycaprylylsilane, Fragrance(Parfum), Iron Oxides (CI 77499), Ethylhexylglycerin, Adenosine, Polysorbate 60, Disodium EDTA, Sorbitan Isostearate, Lavandula Angustifolia (Lavender) Water, Rosmarinus Officinalis (Rosemary) Leaf Water, Anthemis Nobilis Flower Water, Aloe Barbadensis Leaf Juice, Water, Imperata Cylindrica Root Extract, PEG-8, Butylene Glycol, Cassia Angustifolia Seed Polysaccharide, Aesculus Hippocastanum (Horse Chestnut) Extract, Alcohol, Benzyl Alcohol, Ethyl Hexanediol, Caprylyl Glycol, Methylparaben, 1,2-Hexanediol, Dehydroacetic Acid, Potassium Sorbate, Caprylhydroxamic Acid, Butylparaben, Ethylparaben, Propylparaben, Isobutylparaben, Tropolone

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

CAUTION

WARNINGS SECTION

CAUTION:
If redness or irritation occurs, discontinue use and consult a dermatologist. Do not use on broken skin. For external use only. Replace the cap after use. Keep out of reach of children. Do not expose to heat or direct sunlight. Do not store at high temperatures. Avoid contact with eyes.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

How to Use

INDICATIONS & USAGE SECTION

How to Use: Moisturize your skin after your daily skincare routine and use as a substitute for BB Cream to naturally cover blemishes and correct your skin tone.

Dosage & Administration

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration:
This water-based mild formula is specially designed for men to complete a flawless, naturally glowing healthy complexion while preventing greasiness and helping improve skin's moisture balance without darkening.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Dipropylene GlycolINACTIVE INGREDIENTE107L85C401
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69106-09069106-090-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTISALATE4X49Y0596WACTIB
Water059QF0KO0RIACT
Dipropylene GlycolE107L85C40IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
Dipropylene GlycolDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
eb17f988-7d9e-4079-bbeb-4d19dfbf545e1aabcd3c-10ae-48d3-aa8d-d5e296f8ebc82014-08-13WarningsExact identifier
spl id: eb17f988-7d9e-4079-bbeb-4d19dfbf545e
spl set id: 1aabcd3c-10ae-48d3-aa8d-d5e296f8ebc8

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.